Canonical Allele Identifier: CA645570177

Gene: GRIN2A

Linked Data

• COSMIC: COSM5611302

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.9763447_9763448delinsAA , CM000678.2:g.9763447_9763448delinsAA	GRCh38
NC_000016.9:g.9857304_9857305delinsAA , CM000678.1:g.9857304_9857305delinsAA	GRCh37
NC_000016.8:g.9764805_9764806delinsAA	NCBI36
NG_011812.1:g.424307_424308delinsTT
NG_011812.2:g.424307_424308delinsTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330684.4:c.4096_4097delinsTT MANE Select	ENSP00000332549.3:p.Pro1366Phe
ENST00000535259.6:c.3302-20_3302-19delinsTT	ENSP00000441572.3:n.3302-20_3302-19delinsTT
ENST00000636273.2:n.3366-20_3366-19delinsTT
ENST00000674742.1:c.3625_3626delinsTT	ENSP00000502200.1:p.Pro1209Phe
ENST00000675398.1:c.*1466_*1467delinsTT	ENSP00000502752.1:n.*1466_*1467delinsTT
ENST00000330684.3:c.4096_4097delinsTT	ENSP00000332549.3:p.Pro1366Phe
ENST00000396573.6:c.4096_4097delinsTT	ENSP00000379818.2:p.Pro1366Phe
ENST00000396575.6:c.3685_3686delinsTT	ENSP00000379820.3:p.Pro1229Phe
ENST00000461292.3:n.3412-20_3412-19delinsTT
ENST00000535259.5:c.3362-20_3362-19delinsTT	ENSP00000441572.2:n.3362-20_3362-19delinsTT
ENST00000562109.5:c.3773-20_3773-19delinsTT	ENSP00000454998.1:n.3773-20_3773-19delinsTT
NM_000833.4:c.4096_4097delinsTT	NP_000824.1:p.Pro1366Phe
NM_001134407.2:c.4096_4097delinsTT	NP_001127879.1:p.Pro1366Phe
NM_001134408.2:c.3773-20_3773-19delinsTT	NP_001127880.1:n.3773-20_3773-19delinsTT
XM_011522456.1:c.3937_3938delinsTT	XP_011520758.1:p.Pro1313Phe
XM_011522457.1:c.3838_3839delinsTT	XP_011520759.1:p.Pro1280Phe
XM_011522458.1:c.3625_3626delinsTT	XP_011520760.1:p.Pro1209Phe
XM_011522459.1:c.3625_3626delinsTT	XP_011520761.1:p.Pro1209Phe
XM_011522460.1:c.3625_3626delinsTT	XP_011520762.1:p.Pro1209Phe
XM_011522461.1:c.3773-20_3773-19delinsTT	XP_011520763.1:n.3773-20_3773-19delinsTT
XM_011522458.3:c.3625_3626delinsTT	XP_011520760.1:p.Pro1209Phe
XM_011522461.3:c.3773-20_3773-19delinsTT	XP_011520763.1:n.3773-20_3773-19delinsTT
XM_017023172.1:c.4252_4253delinsTT	XP_016878661.1:p.Pro1418Phe
XM_017023173.1:c.3929-20_3929-19delinsTT	XP_016878662.1:n.3929-20_3929-19delinsTT
NM_001134407.3:c.4096_4097delinsTT MANE Select	NP_001127879.1:p.Pro1366Phe
NM_000833.5:c.4096_4097delinsTT	NP_000824.1:p.Pro1366Phe